RHO

rhodopsin
OMIM: 180380, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green RHO in Mendeliome Version 1.1902	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Night blindness, congenital stationary, autosomal dominant 1, MIM# 610445 Retinitis pigmentosa 4, autosomal dominant or recessive, MIM# 613731
Green RHO in Retinitis pigmentosa_Autosomal Recessive/X-linked Level 2: Ophthalmological disorders Version 0.147 Component of the following Super Panels: Retinal Disorders Superpanel Retinitis Pigmentosa Superpanel	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Retinitis pigmentosa 4, autosomal dominant or recessive, 613731 Retinitis punctata albescens Congenital Stationary Night Blindness
Green RHO in Retinitis pigmentosa_Autosomal Dominant Level 2: Ophthalmological disorders Version 0.57 Component of the following Super Panels: Retinal Disorders Superpanel Retinitis Pigmentosa Superpanel	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Retinitis pigmentosa 4, autosomal dominant or recessive, 613731 Congenital Stationary Night Blindness
Green RHO in Congenital Stationary Night Blindness Level 2: Ophthalmological disorders Version 0.23 Component of the following Super Panels: Retinal Disorders Superpanel	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Retinitis punctata albescens Retinitis pigmentosa Night blindness, congenital stationary autosomal dominant 1
Red RHO in Congenital nystagmus Level 2: Ophthalmological disorders Version 1.21	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Red Royal Melbourne Hospital Victorian Clinical Genetics Services Phenotypes Night blindness, congenital stationary, autosomal dominant 1, MIM# 610445 Retinitis pigmentosa 4, autosomal dominant or recessive, MIM# 613731